open access publication

Article, 2024

Ultra-fast label-free quantification and comprehensive proteome coverage with narrow-window data-independent acquisition

Nature Biotechnology, ISSN 1087-0156, 10.1038/s41587-023-02099-7

Contributors

Guzman U.H. 0000-0003-1665-7659 [1] Martinez-Val A. 0000-0002-8784-3822 [1] Ye Z. 0000-0001-8829-6579 [1] [2] Damoc E. [3] Arrey T.N. [3] Pashkova A. [3] Renuse S. [4] Denisov E. [3] Petzoldt J. [3] Peterson A.C. [3] Harking F.S. 0000-0001-5553-1421 [1] Ostergaard O. 0000-0003-3160-8548 [1] Rydbirk R. 0000-0002-4670-7533 [5] Aznar S. 0000-0001-7940-6246 [6] Stewart H. [3] Xuan Y. 0000-0001-9132-2643 [3] Hermanson D. [4] Horning S. [3] Hock C. [3] Makarov A. 0000-0002-7046-6709 [3] Zabrouskov V. [4] Olsen J.V. 0000-0002-4747-4938 (Corresponding author) [1]

Affiliations

  1. [1] University of Copenhagen
  2. [NORA names: KU University of Copenhagen; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Chinese Academy of Medical Sciences
  4. [NORA names: China; Asia, East];
  5. [3] Thermo Fisher Scientific
  6. [NORA names: Germany; Europe, EU; OECD];
  7. [4] Thermo Fisher Scientific
  8. [NORA names: United States; America, North; OECD];
  9. [5] University of Southern Denmark
  10. [NORA names: SDU University of Southern Denmark; University; Denmark; Europe, EU; Nordic; OECD];

Abstract

Mass spectrometry (MS)-based proteomics aims to characterize comprehensive proteomes in a fast and reproducible manner. Here we present the narrow-window data-independent acquisition (nDIA) strategy consisting of high-resolution MS1 scans with parallel tandem MS (MS/MS) scans of ~200 Hz using 2-Th isolation windows, dissolving the differences between data-dependent and -independent methods. This is achieved by pairing a quadrupole Orbitrap mass spectrometer with the asymmetric track lossless (Astral) analyzer which provides >200-Hz MS/MS scanning speed, high resolving power and sensitivity, and low-ppm mass accuracy. The nDIA strategy enables profiling of >100 full yeast proteomes per day, or 48 human proteomes per day at the depth of ~10,000 human protein groups in half-an-hour or ~7,000 proteins in 5 min, representing 3Ă— higher coverage compared with current state-of-the-art MS. Multi-shot acquisition of offline fractionated samples provides comprehensive coverage of human proteomes in ~3 h. High quantitative precision and accuracy are demonstrated in a three-species proteome mixture, quantifying 14,000+ protein groups in a single half-an-hour run.

Funders

  • Innovation Fund for Medical Sciences
  • NCTIB Fund for the R&D Platform for Cell and Gene Therapy
  • Horizon 2020 Framework Programme
  • Novo Nordisk Fonden
  • European Research Council
  • Novo Nordisk Foundation’s Copenhagen Bioscience
  • Non-profit Central Research Institute Fund of the Chinese Academy of Medical Sciences
  • Chinese Academy of Medical Sciences

Data Provider: Elsevier